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Looking for US-based regulatory affairs consultant with oncology and biotech background

  • Clinical development and testing, clinical CRO, Regulatory services - CMC writing - medical writing, Consulting - strategy and development
  • Biopharmaceuticals
  • North America
  • 08/23/2013


We are a EU-based biotech company developing mAb and look for a US based RA consultant who could support us with respect to our programme in order to understand and prepare for US-specific interests, questions and enquiries. We want to be prepared specifically to comply with US-specific clinical demands and understand what requirements FDA has in this field of biotech products for oncology in early development and marketing phase.

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